Clomiphene citrate medication for infertility and risk of stillbirth or neonatal death: a population-based cohort study.

clomiphene citrate neonatal death perinatal death polycystic ovary syndrome stillbirth

Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
22 Oct 2024
Historique:
received: 13 08 2024
revised: 10 10 2024
accepted: 22 10 2024
medline: 22 10 2024
pubmed: 22 10 2024
entrez: 22 10 2024
Statut: aheadofprint

Résumé

Women achieving pregnancy with infertility treatment may be at increased risk of stillbirth and neonatal death. To assess associations between clomiphene citrate (CC) use and perinatal death. Whole of population data linkage cohort. South Australia. All women giving birth between July 2003 and December 2015 (n=242,077). All births of at least 20 weeks were linked to government records of dispensed medications. A pregnancy was considered exposed to CC if a prescription was dispensed from 90 days before through to the end of a conception window. Descriptive statistics for stillbirths and neonatal deaths were stratified by multiplicity. For singletons, multivariable logistic regression models were used to examine the association of CC exposure with the combined outcome of perinatal death. Stillbirths and neonatal deaths (with 28 days of birth) combined as perinatal deaths. Among singletons, the prevalence of stillbirth was 6.6 per 1,000 births, with neonatal deaths of 2.1 per 1,000 live births. Among singletons conceived with CC, stillbirth and neonatal death had prevalence of 10.2 and 3.1 per 1,000, respectively. For the combined outcome of perinatal death, the odds ratio was 1.54 (95% confidence interval 1.15, 2.07), stable upon adjustment for factors conveying biological (e.g. obesity, pre-gestational diabetes) and social (e.g. disadvantage) risks for perinatal death. Risk of perinatal death may be increased in pregnancies that follow use of CC. While established confounding factors related to infertility were taken into account, there may be some residual contribution of underlying infertility.

Identifiants

pubmed: 39437266
pii: 7831527
doi: 10.1210/clinem/dgae741
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the Endocrine Society.

Auteurs

Vivienne Moore (V)

School of Public Health, The University of Adelaide, South Australia.
Robinson Research Institute, The University of Adelaide, South Australia.

Alice Rumbold (A)

Robinson Research Institute, The University of Adelaide, South Australia.
South Australian Health and Medical Research Institute, South Australia.

Renae Fernandez (R)

Robinson Research Institute, The University of Adelaide, South Australia.
Adelaide Medical School, The University of Adelaide, South Australia.

Heather McElroy (H)

Adelaide Medical School, The University of Adelaide, South Australia.

Lynette Moore (L)

Adelaide Medical School, The University of Adelaide, South Australia.
SA Pathology, Women's and Children's Hospital, Adelaide, South Australia.

Lynne Giles (L)

School of Public Health, The University of Adelaide, South Australia.
Robinson Research Institute, The University of Adelaide, South Australia.

Luke Grzeskowiak (L)

South Australian Health and Medical Research Institute, South Australia.
College of Medicine and Public Health, Flinders University, South Australia.

Elizabeth Roughead (E)

Quality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, South Australia.

Michael Stark (M)

Robinson Research Institute, The University of Adelaide, South Australia.
Adelaide Medical School, The University of Adelaide, South Australia.

Darryl Russell (D)

Robinson Research Institute, The University of Adelaide, South Australia.
School of Biomedicine, The University of Adelaide, South Australia.

Michael Davies (M)

Robinson Research Institute, The University of Adelaide, South Australia.
Adelaide Medical School, The University of Adelaide, South Australia.

Classifications MeSH